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CAS 162607-17-2

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5-bromo-2-thienylboronic acid

Description:
5-Bromo-2-thienylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thiophene ring that is substituted with a bromine atom. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of the bromine atom enhances its reactivity, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. Additionally, the thiophene moiety contributes to its electronic properties, allowing for potential applications in organic electronics and materials science. The compound is also of interest in medicinal chemistry due to its potential biological activity, as boronic acids can interact with biological targets, including enzymes and receptors. Proper handling and storage are essential, as with many organoboron compounds, to maintain stability and prevent degradation.
Formula:C4H4BBrO2S
InChI:InChI=1/C4H4BBrO2S/c6-4-2-1-3(9-4)5(7)8/h1-2,7-8H
SMILES:c1cc(Br)sc1B(O)O
Synonyms:
  • 5-Bromothiophene-2-boronic acid
  • (5-Bromothiophen-2-Yl)Boronic Acid
  • 5-Bromo-2-thiopheneboronic acid
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